1mrq

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(New page: 200px<br /> <applet load="1mrq" size="450" color="white" frame="true" align="right" spinBox="true" caption="1mrq, resolution 1.59&Aring;" /> '''Crystal structure o...)
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<applet load="1mrq" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1mrq, resolution 1.59&Aring;" />
caption="1mrq, resolution 1.59&Aring;" />
'''Crystal structure of human 20alpha-HSD in ternary complex with NADP and 20alpha-hydroxy-progesterone'''<br />
'''Crystal structure of human 20alpha-HSD in ternary complex with NADP and 20alpha-hydroxy-progesterone'''<br />
==Overview==
==Overview==
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Human 20alpha-hydroxysteroid dehydrogenase (h20alpha-HSD; AKR1C1), catalyzes the transformation of progesterone (Prog) into, 20alpha-hydroxy-progesterone (20alpha-OHProg). Although h20alpha-HSD, shares 98% sequence identity with human type 3 3alpha-HSD (h3alpha-HSD3, AKR1C2), these two enzymes differ greatly in their activities. In order to, explain these differences, we have solved the crystal structure of, h20alpha-HSD in a ternary complex with NADP(+) and 20alpha-OHProg at 1.59A, resolution. The steroid is stabilized by numerous hydrophobic interactions, and a hydrogen bond between its O20 and the N(epsilon ) atom of His222., This new interaction prevents the formation of a hydrogen bond with the, cofactor, as seen in h3alpha-HSD3 ternary complexes. By combining, structural, direct mutagenesis and kinetic studies, we found that the, H(222)I substitution decreases the K(m) value for the cofactor 95-fold., With these results, we hypothesize that the rotation of the lateral chain, of His222 could be a mediating step between the transformation of Prog and, the release of the cofactor. Moreover, crystal structure analysis and, direct mutagenesis experiments lead us to identify a new residue involved, in the binding of Prog. Indeed, the R(304)L substitution leads to a, 65-fold decrease in the K(m) value for Prog reduction. We thus propose, that Prog is maintained in a new steroid-binding site composed mainly of, residues found in the carboxy-terminal region of the protein.
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Human 20alpha-hydroxysteroid dehydrogenase (h20alpha-HSD; AKR1C1) catalyzes the transformation of progesterone (Prog) into 20alpha-hydroxy-progesterone (20alpha-OHProg). Although h20alpha-HSD shares 98% sequence identity with human type 3 3alpha-HSD (h3alpha-HSD3, AKR1C2), these two enzymes differ greatly in their activities. In order to explain these differences, we have solved the crystal structure of h20alpha-HSD in a ternary complex with NADP(+) and 20alpha-OHProg at 1.59A resolution. The steroid is stabilized by numerous hydrophobic interactions and a hydrogen bond between its O20 and the N(epsilon ) atom of His222. This new interaction prevents the formation of a hydrogen bond with the cofactor, as seen in h3alpha-HSD3 ternary complexes. By combining structural, direct mutagenesis and kinetic studies, we found that the H(222)I substitution decreases the K(m) value for the cofactor 95-fold. With these results, we hypothesize that the rotation of the lateral chain of His222 could be a mediating step between the transformation of Prog and the release of the cofactor. Moreover, crystal structure analysis and direct mutagenesis experiments lead us to identify a new residue involved in the binding of Prog. Indeed, the R(304)L substitution leads to a 65-fold decrease in the K(m) value for Prog reduction. We thus propose that Prog is maintained in a new steroid-binding site composed mainly of residues found in the carboxy-terminal region of the protein.
==Disease==
==Disease==
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==About this Structure==
==About this Structure==
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1MRQ is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with NAP, STR and BME as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/20-alpha-hydroxysteroid_dehydrogenase 20-alpha-hydroxysteroid dehydrogenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.149 1.1.1.149] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1MRQ OCA].
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1MRQ is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=NAP:'>NAP</scene>, <scene name='pdbligand=STR:'>STR</scene> and <scene name='pdbligand=BME:'>BME</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/20-alpha-hydroxysteroid_dehydrogenase 20-alpha-hydroxysteroid dehydrogenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.149 1.1.1.149] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1MRQ OCA].
==Reference==
==Reference==
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[[Category: Breton, R.]]
[[Category: Breton, R.]]
[[Category: Cantin, L.]]
[[Category: Cantin, L.]]
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[[Category: Couture, J.F.]]
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[[Category: Couture, J F.]]
[[Category: Labrie, F.]]
[[Category: Labrie, F.]]
[[Category: Legrand, P.]]
[[Category: Legrand, P.]]
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[[Category: ternary complex]]
[[Category: ternary complex]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 18:14:21 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:58:22 2008''

Revision as of 11:58, 21 February 2008


1mrq, resolution 1.59Å

Drag the structure with the mouse to rotate

Crystal structure of human 20alpha-HSD in ternary complex with NADP and 20alpha-hydroxy-progesterone

Contents

Overview

Human 20alpha-hydroxysteroid dehydrogenase (h20alpha-HSD; AKR1C1) catalyzes the transformation of progesterone (Prog) into 20alpha-hydroxy-progesterone (20alpha-OHProg). Although h20alpha-HSD shares 98% sequence identity with human type 3 3alpha-HSD (h3alpha-HSD3, AKR1C2), these two enzymes differ greatly in their activities. In order to explain these differences, we have solved the crystal structure of h20alpha-HSD in a ternary complex with NADP(+) and 20alpha-OHProg at 1.59A resolution. The steroid is stabilized by numerous hydrophobic interactions and a hydrogen bond between its O20 and the N(epsilon ) atom of His222. This new interaction prevents the formation of a hydrogen bond with the cofactor, as seen in h3alpha-HSD3 ternary complexes. By combining structural, direct mutagenesis and kinetic studies, we found that the H(222)I substitution decreases the K(m) value for the cofactor 95-fold. With these results, we hypothesize that the rotation of the lateral chain of His222 could be a mediating step between the transformation of Prog and the release of the cofactor. Moreover, crystal structure analysis and direct mutagenesis experiments lead us to identify a new residue involved in the binding of Prog. Indeed, the R(304)L substitution leads to a 65-fold decrease in the K(m) value for Prog reduction. We thus propose that Prog is maintained in a new steroid-binding site composed mainly of residues found in the carboxy-terminal region of the protein.

Disease

Known disease associated with this structure: Obesity, hyperphagia, and developmental delay OMIM:[600450]

About this Structure

1MRQ is a Single protein structure of sequence from Homo sapiens with , and as ligands. Active as 20-alpha-hydroxysteroid dehydrogenase, with EC number 1.1.1.149 Full crystallographic information is available from OCA.

Reference

Human 20alpha-hydroxysteroid dehydrogenase: crystallographic and site-directed mutagenesis studies lead to the identification of an alternative binding site for C21-steroids., Couture JF, Legrand P, Cantin L, Luu-The V, Labrie F, Breton R, J Mol Biol. 2003 Aug 15;331(3):593-604. PMID:12899831

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